## Abstract ## Purpose To investigate the diffusion tensor properties of the human optic nerve in vivo using a non‐Carr‐Purcell‐Meiboom‐Gill (CPMG) fast spin echo (FSE) sequence. ## Materials and Methods This non‐CPMG FSE sequence, which is based on a quadratic phase modulation of the refocusing
On the application of a non-CPMG single-shot fast spin-echo sequence to diffusion tensor MRI of the human brain
✍ Scribed by Mark E. Bastin; Patrick Le Roux
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 785 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
The strong sensitivity of Carr-Purcell-Meiboom-Gill (CPMG) fast spin-echo (FSE) sequences, such as rapid acquisition with relaxation enhancement (RARE), to the phase of the prepared transverse magnetization means that artifact-free single-shot diffusion-weighted images can currently only be obtained with a 30-50% reduction in the signal-to-noise ratio (SNR). However, this phase sensitivity and signal loss can be addressed in FSE sequences that use quadratic phase modulation of the radiofrequency (RF) refocusing pulses to generate a sustained train of stable echoes. Here the first application of such a non-CPMG single-shot FSE (ssFSE) sequence to diffusion tensor MR imaging (DT-MRI) of the human brain is described. This approach provides high SNR diffusion-weighted images that have little or no susceptibility to poor B(0) magnetic field homogeneity and the strong eddy currents typically present in DT-MRI experiments.
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## Abstract The accuracy of water T2 maps generated from a fast spin‐echo (FSE) sequence was compared with data obtained by conventional single and multi‐echo spin‐echo pulse sequences using a commercial gel phantom. Spatially localized stimulated echo acquisition mode (STEAM) proton spectroscopy w